D57 Sickle-cell disorders

(Sickle-cell disorders )

Rare males and females disease from the section "Haemolytic anaemias". Causes not a significant loss of workdays. May be the cause of death.

32 830 people were diagnosed with Sickle-cell disorders

97 died with a diagnosis of Sickle-cell disorders

0 % disease mortality Sickle-cell disorders

Clinical picture Diagnostics Treatment

Sickle-cell disorders is diagnosed to men at 35.63% more often than women

18 897

Men are diagnosed with Sickle-cell disorders. There were no deaths.

0 %

mortality in men with disease Sickle-cell disorders

13 933

Women are diagnosed with Sickle-cell disorders For 97 of these, this diagnosis is fatal.

0.01 %

mortality in women with disease Sickle-cell disorders

Risk group for the disease Sickle-cell disorders men aged 10-14 and women aged10-14

The disease is most common in men aged 10-14

In men, the disease is least likely to occur at the age of 60-64, 90+

In women, the disease is least likely to occur at the age of 50-54, 90+

The disease is most common in women aged 10-14

Features of the disease Sickle-cell disorders

Absence or low individual and social danger

Diagnostics

Standard for diagnosing the disease Sickle-cell disorders not found

Diagnosis Sickle-cell disorders on the 3 place in the frequency of diseases in the rubric of other Haemolytic anaemias diseases

Most common:

Acquired haemolytic anaemia Other hereditary haemolytic anaemias Sickle-cell disorders

Sickle-cell disorders disease on the 5 most dangerous disease in the category of other Haemolytic anaemias diseases

Most dangerous:

Thalassaemia Anaemia due to enzyme disorders Acquired haemolytic anaemia

Treatment

The standard for the treatment of the disease Sickle-cell disorders is not is established

5 days required for doctors in inpatient treatment

2 hour(s) is required for outpatient treatment

0 medical procedures are provided for the treatment of Sickle-cell disorders

Specific forms of the disease

D57.0: Sickle-cell anaemia with crisis

D57.1: Sickle-cell anaemia without crisis

D57.2: Double heterozygous sickling disorders

D57.3: Sickle-cell trait

D57.8: Other sickle-cell disorders

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